Canonical Allele Identifier: CA1355986160

Gene: GLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33018467G= , CM000665.2:g.33018467G=	GRCh38
NC_000003.11:g.33059959G= , CM000665.1:g.33059959G=	GRCh37
NC_000003.10:g.33034963G=	NCBI36
NG_009005.1:g.83736C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307363.10:c.1328C= MANE Select	ENSP00000306920.4:p.Ala443=
ENST00000307363.9:c.1328C=	ENSP00000306920.4:p.Ala443=
ENST00000307377.12:c.935C=	ENSP00000305920.8:p.Ala312=
ENST00000399402.7:c.1238C=	ENSP00000382333.2:p.Ala413=
ENST00000461475.5:n.427C=
ENST00000467571.5:n.365C=
ENST00000497796.5:n.580C=
NM_000404.2:c.1328C=	NP_000395.2:p.Ala443=
NM_000404.3:c.1328C=	NP_000395.2:p.Ala443=
NM_001079811.1:c.1238C=	NP_001073279.1:p.Ala413=
NM_001079811.2:c.1238C=	NP_001073279.1:p.Ala413=
NM_001135602.1:c.935C=	NP_001129074.1:p.Ala312=
NM_001135602.2:c.935C=	NP_001129074.1:p.Ala312=
NM_001317040.1:c.1472C=	NP_001303969.1:p.Ala491=
NM_000404.4:c.1328C= MANE Select	NP_000395.3:p.Ala443=
NM_001079811.3:c.1238C=	NP_001073279.2:p.Ala413=
NM_001135602.3:c.935C=	NP_001129074.2:p.Ala312=
NM_001317040.2:c.1472C=	NP_001303969.2:p.Ala491=
NM_001393580.1:c.1328C=	NP_001380509.1:p.Ala443=